Rogers S G, Rhoades M
Proc Natl Acad Sci U S A. 1976 May;73(5):1576-80. doi: 10.1073/pnas.73.5.1576.
Four site-specific endodeoxyribonucleases have been partially purified from extracts of bacteriophage T5-infected Escherichia coli by gel filtration and affinity chromatography on single- and double-stranded DNA. The enzymes were detected and characterized by agarose gel electrophoresis of alkali-denatured digestion products. None of the four is found in uninfected cells. In the presence of a divalent cation, all four endonucleases make ligase-repairable, single-chain interruptions at specific sites in the duplex DNA of several bacteriophages (lambda, T7, and T5) and a mammalian virus (adenovirus 2). These activities are not stimulated by ATP. None of the four is active on single-stranded DNA. The fragments produced by each enzyme from ligase-repaired T5 DNA do not correspond to those derived from mature T5 DNA. Each of the enzymes is able to cleave the intact strand of T5 DNA.
通过凝胶过滤以及在单链和双链DNA上进行亲和层析,已从感染噬菌体T5的大肠杆菌提取物中部分纯化出四种位点特异性内切脱氧核糖核酸酶。通过对碱变性消化产物进行琼脂糖凝胶电泳来检测和表征这些酶。在未感染的细胞中未发现这四种酶中的任何一种。在二价阳离子存在的情况下,所有四种内切核酸酶都会在几种噬菌体(λ噬菌体、T7噬菌体和T5噬菌体)以及一种哺乳动物病毒(腺病毒2)的双链DNA的特定位点产生可被连接酶修复的单链中断。这些活性不受ATP的刺激。这四种酶中没有一种对单链DNA有活性。每种酶从连接酶修复的T5 DNA产生的片段与从成熟T5 DNA衍生的片段不对应。每种酶都能够切割T5 DNA的完整链。